Canonical Allele Identifier: CA383970784
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 1740272
ClinVar RCV Id: RCV002333691

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718278C>A , CM000674.2:g.12718278C>A GRCh38
NC_000012.11:g.12871212C>A , CM000674.1:g.12871212C>A GRCh37
NC_000012.10:g.12762479C>A NCBI36
NG_016341.1:g.5911C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.439C>A ENSP00000507272.1:p.Gln147Lys
ENST00000682620.1:n.1631-547C>A
ENST00000684771.1:n.585-547C>A
ENST00000228872.9:c.439C>A MANE Select ENSP00000228872.4:p.Gln147Lys
ENST00000228872.8:c.439C>A ENSP00000228872.4:p.Gln147Lys
ENST00000396340.1:c.439C>A ENSP00000379629.1:p.Gln147Lys
ENST00000442489.1:c.193+225C>A ENSP00000407597.1:n.193+225C>A
ENST00000477087.1:n.155-547C>A
NM_004064.4:c.439C>A NP_004055.1:p.Gln147Lys
NM_004064.5:c.439C>A MANE Select NP_004055.1:p.Gln147Lys